Collecting information
Organizing data
Perform the day-to-day administrative activities of clinical research trial programs. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments such as neonatology, cardiology, radiology etc. Collect, enter and disseminate
Clinical Research Assistant I to support two newly funded, community-engaged research projects focused on health disparities and social determinants of health in Milwaukee, Wisconsin. The ideal candidate is motivated by people-centered work, values collaboration, and is committed to supporting resea
Collect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized database. Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Under the direction of the study coordinator
Building relationships and developing a customer base of alternate site physician offices as well as hospital based practices Making new calls on a daily basis to develop new customers Working with manufacturers to present products to the physician community Prepare and deliver quotations for produc
Perform the day-to-day administrative activities of clinical research trial programs. Assure compliance with all relevant IRB and other regulatory agency requirements. Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Perform the day-to-day administrative activities of the clinical research trials program. Assist in the evaluation and writing of research protocols. Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Perform the day-to-day administrative activities of the clinical research trials program. Assist in the evaluation and writing of research protocols. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutio
Perform the day-to-day administrative activities of clinical research trial programs. At MCW all of our endeavors, from our internal operations to our interactions with our partners, are driven by our shared organizational values: Caring - Collaborative - Curiosity - Inclusive - Integrity - Respect.
Assist CTO research team members in screening, recruiting and enrolling patients into clinical trials. Collect required data from study participants, and enter into clinical research forms and into computerized databases. Under general supervision, assist in various administrative and data collectio
Account Rep II on the Medicaid team,. Apply extensive knowledge of multiple contracts, agreements and government guidelines/regulations to submit, post, research and/or resolve accounts or claims. EPIC experience and Medical Billing/Follow-up experience.
Under direct supervision, perform routine administrative duties in support of clinical research studies. The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. Accurately enter research data into specified programs or databases.
Under direct supervision, perform routine administrative duties in support of clinical research studies. Accurately enter research data into specified programs or databases. Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental.
Under direct supervision, perform routine administrative duties in support of clinical research studies. Accurately enter research data into specified programs or databases. Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental.
Assist in the evaluation and writing of research protocols. Perform the day-to-day administrative activities of the clinical research trials program. Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators
Perform the day-to-day administrative activities of the clinical research trials program. Assist in the evaluation and writing of research protocols. Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental.
Coordinate the day-to-day administrative activities of the clinical research trials program. Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators. The Medical College of Wisconsin (MCW) is an Equal Oppo
Perform the day-to-day administrative activities of clinical research trial programs. Assure compliance with all relevant IRB and other regulatory agency requirements. Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental.
The Clinical Research Coordinator II will support a multiyear NIHfunded R01 study in the Department of Pediatrics, Section of Neonatology. Contribute to the evaluation and writing of research protocols in collaboration with the PI. Knowledge of clinical research processes, documentation, and records